Member Bibliography/Bibliografía de Miembros
Esta página presenta todas las publicaciones personales que los miembros de CienciaPR han subido a sus perfiles. También puedes ver todos los autores en esta colección de publicaciones o todas las palabras claves contenidas en la colección.
«Ocular Findings in Patients with the Hermansky-Pudlak Syndrome (Types 1 and 3).», Ophthalmic Genet, 2014.
, «Pharmacogenetic association study of warfarin safety endpoints in Puerto Ricans.», P R Health Sci J, vol. 33, n.º 3, pp. 97-104, 2014.
, «Pharmacogenetics of drug-metabolizing enzymes in US Hispanics.», Drug Metabol Drug Interact, 2014.
, , «CYP2D6's functional status associated with the length of hospitalization stay in psychiatric patients: a twist in the tale or evidence that matters?», Biomark Med, vol. 7, n.º 6, pp. 913-4, 2013.
, «A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).», Biochim Biophys Acta, vol. 1833, n.º 3, pp. 468-78, 2013.
, «Frequencies of Functional Polymorphisms in Three Pharmacokinetic Genes of Clinical Interest within the Admixed Puerto Rican Population.», J Pharmacogenomics Pharmacoproteomics, vol. 4, n.º 113, 2013.
, «Ocular findings in patients with oculocutaneous albinism type ia with G47D tyrosinase gene mutation in Puerto Rico: a case report.», Bol Asoc Med P R, vol. 105, n.º 2, pp. 62-4, 2013.
, «Development of a pharmacogenetic-guided warfarin dosing algorithm for Puerto Rican patients.», Pharmacogenomics, vol. 13, n.º 16, pp. 1937-50, 2012.
, «Dysregulation of macrophage-secreted cathepsin B contributes to HIV-1-linked neuronal apoptosis.», PLoS One, vol. 7, n.º 5, p. e36571, 2012.
, «Prediction of warfarin dose reductions in Puerto Rican patients, based on combinatorial CYP2C9 and VKORC1 genotypes.», Ann Pharmacother, vol. 46, n.º 2, pp. 208-18, 2012.
, «Asymptomatic child heterozygous for hemoglobin S and hemoglobin Pôrto Alegre.», Pediatr Blood Cancer, vol. 56, n.º 3, pp. 458-9, 2011.
, «Nonsense mutations of the bHLH transcription factor TWIST2 found in Setleis Syndrome patients cause dysregulation of periostin.», Int J Biochem Cell Biol, vol. 43, n.º 10, pp. 1523-31, 2011.
, «Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico.», J Pediatr, vol. 159, n.º 4, pp. 623-7.e1, 2011.
, «Redundant or separate entities?--roles of Twist1 and Twist2 as molecular switches during gene transcription.», Nucleic Acids Res, vol. 39, n.º 4, pp. 1177-86, 2011.
, «CYP2C9 and VKORC1 genotypes in Puerto Ricans: A case for admixture-matching in clinical pharmacogenetic studies.», Clin Chim Acta, vol. 411, n.º 17-18, pp. 1306-11, 2010.
, «Homozygous nonsense mutations in TWIST2 cause Setleis syndrome.», Am J Hum Genet, vol. 87, n.º 2, pp. 289-96, 2010.
, «MTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers.», Int J Genet Mol Biol, vol. 2, n.º 3, pp. 43-47, 2010.
, «Newborn screening for hermansky-pudlak syndrome type 3 in Puerto Rico.», J Pediatr Hematol Oncol, vol. 32, n.º 6, pp. 448-53, 2010.
, «Recombinant hemoglobin II from Lucina pectinata: a large-scale method for hemeprotein expression in E. coli.», Protein J, vol. 29, n.º 2, pp. 143-51, 2010.
, «Restricted HIV-1 replication in placental macrophages is caused by inefficient viral transcription.», J Leukoc Biol, vol. 87, n.º 4, pp. 633-6, 2010.
, «Factors controlling the reactivity of hydrogen sulfide with hemeproteins.», Biochemistry, vol. 48, n.º 22, pp. 4881-94, 2009.
, «For the patient. DNA makeup of Hispanic persons should be determined before warfarin prescription.», Ethn Dis, vol. 19, n.º 4, pp. 479-80, 2009.
, «Physiogenomic analysis of the Puerto Rican population.», Pharmacogenomics, vol. 10, n.º 4, pp. 565-77, 2009.
, «Prevalence of combinatorial CYP2C9 and VKORC1 genotypes in Puerto Ricans: implications for warfarin management in Hispanics.», Ethn Dis, vol. 19, n.º 4, pp. 390-5, 2009.
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